BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MCKESSON BRANDS

    MDR report key: 23389882 · Received October 27, 2025

    Report

    Report Number
    1451040-2025-00100
    Event Type
    Malfunction
    Date Received
    October 27, 2025
    Date of Event
    October 8, 2025
    Report Date
    October 27, 2025
    Manufacturer
    HARSORIA HEALTHCARE
    Product Code
    QOI
    UDI-DI
    10612479267487
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    NV, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    IT WAS REPORTED BY THE CUSTOMER THAT BLOOD LEAKED DUE TO SAFETY COVER NOT SLIDING OVER NEEDLE. NO INFORMATION WAS RECEIVED REGARDING ANY SERIOUS INJURY AS A RESULT OF THIS PRODUCT ISSUE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2427813 MCKESSON BRANDS CATHETER, IV SFTY SLIDING STR PNK 20GX1" QOI HARSORIA HEALTHCARE 4113/0685 10612479267487

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown